Bioinorganic Chemistry and Applications

Bioinorganic Chemistry and Applications / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 5360361 |

Da-Wei Li, Lei Luo, Peng-Fei Lv, Qing-Qing Wang, Ke-Yu Lu, An-Fang Wei, Qu-Fu Wei, "Synthesis of Polydopamine Functionalized Reduced Graphene Oxide-Palladium Nanocomposite for Laccase Based Biosensor", Bioinorganic Chemistry and Applications, vol. 2016, Article ID 5360361, 10 pages, 2016.

Synthesis of Polydopamine Functionalized Reduced Graphene Oxide-Palladium Nanocomposite for Laccase Based Biosensor

Academic Editor: Luigi Casella
Received22 Apr 2016
Accepted14 Jun 2016
Published05 Jul 2016


Graphene based 2D nanomaterials have attracted increasing attention in biosensing application due to the outstanding physicochemical properties of graphene. In this work, palladium nanoparticles (Pd) loaded reduced graphene oxide (rGO) hybrid (rGO-Pd) was synthesized through a facile method. Laccase (Lac) was immobilized on rGO-Pd by utilizing the self-polymerization of dopamine, which generated polydopamine (PDA). The PDA-Lac-rGO-Pd nanocomposites were further modified on electrode surface to construct novel biosensing platform. The obtained electrochemical biosensor was applied in the detection of catechol, achieving excellent analytic results. Under the optimum condition, this biosensor possessed a linear range from 0.1 µM to 263 µM for catechol detection, the sensitivity reached 18.4 µA mM−1, and the detection limit was as low as 0.03 µM. In addition, the biosensor also showed good repeatability, reproducibility, anti-interference, and stability. Moreover, the novel Lac based biosensor was successfully used in the trace detection of catechol existing in real water environment.

1. Introduction

To our knowledge, phenolic compounds are hazardous and can cause severe health problems to human beings and animals [1]. These harmful compounds, as common industrial raw materials, widely exist in many industries and agriculture [1]. Catechol, as one of numerous phenolic contaminants, is a pivotal industrial chemical agent and can often be found in common foods such as crude beet sugar, coffee, and onion [2]. So, it has attracted a great deal of attention to exploit high-efficient detection methods toward catechol with low detection limit and high sensitivity. Up to now, a variety of catechol detection methods have been invented and applied, like gas chromatography, liquid chromatography, enzyme immunoassays, and so forth [3, 4]. These methods are restricted by their high cost, complicated analytic process, and fixed space location caused by the ponderous analysis instruments. Laccase (Lac) can catalyze the oxidation of phenols, coupled with reduction of O2 to H2O. On basis of this, a large number of Lac based biosensors have been prepared for the detection of catechol [58]. Laccase (Lac) based electrochemical biosensors offer a facile, simple, high-efficient analysis method for the detection of catechol, which is not affected by solution color and can achieve the microminiaturization of analysis apparatus.

Metal nanoparticles have been widely applied in both chemical sensors and biosensors due to their high surface area, high mechanical strength, ultralight weight, rich electronic properties, and excellent chemical and thermal stability [9, 10]. However, abundant metal nanoparticles often aggregate in the fabrication process of biosensor, which extremely affects their electrocatalysis toward substrates. As a result, combination of metal nanoparticles and other conductive materials becomes an effective way to solve the above problem. Graphene was discovered in 2004, which opened a new avenue to electrochemical biosensor research [11]. The unique properties of graphene (high thermal conductivity, fast electron transportation, excellent mechanical flexibility, and biocompatibility) make it become potential application material in electrochemical sensor [12, 13]. Palladium (Pd) nanoparticles loaded graphene oxide (GO) or reduced graphene oxide (rGO), combining their advantages together, have been applied in electrochemical enzyme-free sensors and electrochemical biosensors [1416]. Dopamine (DA), existing in the brains and bodies of animals, is an important neurotransmitter of redox activity. Self-polymerization of DA generates polydopamine (PDA) with good biocompatibility, hydrophilicity, and excellent adhesiveness. Considering these merits of PDA, it has been applied in biosensing and multifunctional coating [1721].

In this work, Pd nanoparticles loaded rGO (rGO-Pd) was synthesized through a facile method. Lac was immobilized on rGO-Pd by utilizing one-pot Lac-catalyzed oxidation of DA in an aqueous suspension containing Lac, rGO-Pd, and DA. The as-prepared PDA-Lac-rGO-Pd composite was used to modify glass carbon electrode (GCE) to construct novel PDA-Lac-rGO-Pd/GCE biosensor. The biosensor was employed to detect harmful phenolic compound (catechol) in water environment and achieved satisfactory analysis results. This study demonstrates that the PDA-Lac-rGO-Pd/GCE biosensor can serve as an effective water environmental monitor and may find potential applications in other research fields, like biofuel cell, biocatalyst, and so forth.

2. Materials and Methods

2.1. Reagents and Materials

Palladium acetate, expanded graphite powder, dopamine (DA), and catechol were purchased from Aladdin Chemical Reagent Co., Ltd. (Shanghai, China). Laccase (Lac, from Trametes, activity ≥ 10 U/mg) was obtained from Sigma-Aldrich and used without further purification. Other chemicals were all purchased from the Sinopharm Group Chemical Reagent Co., Ltd. (Shanghai, China). Acetate buffer solution (0.1 M HAc-NaAc, pH = 5.0) was used as a supporting electrolyte. All aqueous solutions were prepared with deionized water (DIW).

2.2. Characterization

High-resolution transmission electron microscope (TEM, JEOL/JEM-2100, Japan) was used to observe the morphology of rGO-Pd. Powder D8 Advance X-ray diffraction (XRD, Bruker AXS D8) and 3D Nanometer Scale Raman PL Microspectrometer (Tokyo Instruments, Inc., a 785 nm He-Ne laser) were employed to analyze the chemical components of GO, rGO, and rGO-Pd hybrid. The morphology of PDA-Lac-rGO-Pd composite was observed with a Hitachi SU1510 SEM. Fourier transform infrared (FT-IR) spectra were recorded in the range of 500–4000 cm−1 on a Nicolet iS10 FT-IR spectrometer (Thermo Fisher Scientific).

2.3. Preparation of PDA-Lac-rGO-Pd Composite and Biosensors

Prior to use, GO was prepared from expanded graphite powder by Hummers’ method [22]. rGO-Pd was prepared according to the method reported in literature [23]. The fabrication process is shown in Figure 1(a). To begin with, sodium hydroxide solution was added into the prepared GO suspension with a few minutes of sonication at 60°C to obtain rGO suspension [24]. Next, 20 mL of sodium dodecyl sulfate (SDS, 0.1 mol/L) solution was added into the rGO suspension (2.5 mg/mL) followed by 5 min of sonication. After that, 10 mg of palladium acetate was added into the previous solution, and the mixture was refluxed at 110°C with magnetic stirring for 4 h. Lastly, the mixture was washed by deionized water and centrifuged for several times and dried to obtain the rGO-Pd hybrids. Herein, the SDS decomposed to 1-dodecanol when it was heated, which can reduce Pd(OAc)2 to Pd [25].

1 mL rGO-Pd (1.0 mg mL−1) suspension was prepared with the aid of sonication for ca. 5 min. Then, 1 mL Lac solution (1.0 mg mL−1) and 1.0 mL DA solution (2.8 mg mL−1) were successively added in the rGO-Pd suspension under continuous stirring for 3 h. As shown in Figure 1(b), self-polymerization of DA produced polydopamine (PDA), which could wrap the Lac on the surface of rGO-Pd, achieving the immobilization of Lac and the polydopamine functionalization of rGO-Pd. By this way, we obtained the PDA-Lac-rGO-Pd composite.

Before modification, the glass carbon electrode (GCE) was polished to a mirror-like surface with alumina slurry and washed by DIW. Next, the electrode was immersed in ethanol for 5 min with the aid of ultrasonic to remove the adsorbed alumina slurry. After that, the as-prepared electrode was dried in nitrogen. As shown in Figure 1(b), 10 µL of PDA-Lac-rGO-Pd suspension was dropped onto the bare electrode, followed by drying at 4°C in a refrigerator to obtain the PDA-Lac-rGO-Pd/GCE modified electrode. In compared experiments, PDA-Lac/GCE and PDA-Lac-rGO/GCE were prepared by using similar methods, maintaining the equal amounts of DA, Lac, and rGO.

2.4. Electrochemical Measurements

Electrochemical experiments were conducted by using a CHI 660E electrochemical workstation (CH Instruments, Inc., Shanghai, China). A three-electrode cell was employed for electrochemical tests, which contained a GCE, a platinum wire auxiliary electrode, and an Ag/AgCl reference electrode. Before electrochemical experiments, the test solution was bubbled with highly pure nitrogen for 20 min to exclude the influence of oxygen except the amperometric analysis.

3. Results and Discussion

3.1. Characterization

Figure 2(a) shows the transmission electron microscopy (TEM) image of rGO-Pd hybrid. It can be seen that the rGO presents a laminated structure with almost transparent color, which is in accordance with the morphologies reported in literatures [26, 27]. Meanwhile, a large number of small nanoparticles were evenly dispersed on the surface of rGO; only very few aggregation particles can be observed. These nanoparticles may be Pd nanoparticles, which are the reduction products of palladium acetate. As shown in the inset of Figure 2(a), the average diameter of the nanoparticles is ca. 11 nm, so small sizes of Pd nanoparticles are favorable to develop their electrocatalytic properties.

X-ray diffraction (XRD) was employed to investigate the chemical components of GO and rGO-Pd. As shown in Figure 2(b), only one diffraction peak at ca. 11.0° can be seen on the curve for GO; this peak is related to a basal spacing of stacked GO. However, for the XRD pattern for rGO-Pd, there are other five relatively obvious diffraction peaks appearing at 25.0°, 40.1°, 46.6°, 68.1°, and 82.1°, which are corresponded to the (002) plane of graphite and the (111), (200), (220), and (311) face-center cubic lattice planes of Pd, respectively [28, 29]. The XRD result suggested that the GO was chemically reduced to rGO, and Pd nanoparticles were generated on the rGO surface. Raman spectroscopy is usually utilized to characterize the structures of carbon materials. Herein, it was employed to investigate the structure changes of GO, rGO, and rGO-Pd; the result is shown in Figure 2(c). For GO, there are two distinct peaks, appearing at around 1346 cm−1 and 1590 cm−1, which are corresponded to D band and G band, respectively. The D band is relative to the out-of-plane sp3 vibrations of carbons, while the G band can be ascribed to the carbon in-plane sp2 vibrations [30, 31]. The intensity ratio of the D band and G band () reflects the size of sp2-carbon domain and the quantity of defect sites. The value of GO is 0.96, while this value for rGO and rGO-Pd increases to 1.34 and 1.36, indicating that rGO and rGO-Pd harbor more defects than GO, which may be attributed to the smaller size of the rGO sheets [32]. It is noticeable that the spectra of rGO and rGO-Pd are blue shifted in comparison with that of GO; this can be explained by the damage of single and double carbon bonds within sp2 carbon ribbons during the reaction [33]. The Raman spectra indicate the successful reduction of GO. The XRD and Raman spectra characterizations jointly reveal the successful synthesis of rGO-Pd hybrid.

Figure 3(a) displays the scanning electron microscopy (SEM) image of the surface of PDA-Lac-rGO-Pd/GCE. It is manifested that PDA-Lac-rGO-Pd composite forms a porous membrane on the GCE surface. Those “pores” and “ravines” are beneficial to the substrate diffusion. Besides, the “white” nanoparticles on the composite surface may be the excess Pd nanoparticles which fell off from the rGO surface during the synthesis reaction process. Figure 3(b) shows the FT-IR spectra of DA, Lac, PDA-Lac composite, and PDA-Lac-rGO-Pd composite. The spectrum for DA (curve ) is similar to that reported in literature [34]. Those peaks below 1200 cm−1 are related to the in-plane bending vibrations of phenolic groups and CH/CH2 groups, which also can be found in the spectra of PDA-Lac and PDA-Lac-rGO-Pd composites (spectrum (3) and spectrum (4), resp.) [35]. As shown in spectrum , a broad absorption peak at ca. 3423 cm−1 is assigned to NH and OH stretching vibrations in the proteins, which also occurs in curve (c) and curve (d) [36]. The peak at ca. 1630 cm−1 can be ascribed to the characteristic absorption peak of amide I (1700–1600 cm−1), and this peak is shifted to ca. 1605 cm−1 in spectra (c) and (d), indicating the strong interaction reaction between Lac and DA [37]. Notably, spectrum (c) and spectrum (d) show almost same absorption peaks, implying that the addition of rGO-Pd does not affect the composite chemical structure. The FT-IR test result demonstrates the successful synthesis of PDA-Lac-rGO-Pd composite.

3.2. Electrochemical Studies

Electrochemical impedance spectroscopy (EIS) experiments were conducted to investigate the interface resistances of modified electrodes. As shown in Figure 4, the semicircle parts of curves are corresponding to the electron transfer processes occurring on the modified electrodes and the electron transfer resistance of the electrochemical reaction (Ret) is related to the semicircle diameter. Obviously, bare GCE (curve (a)) shows a small semicircle, which almost cannot be observed, implying the negligible interface resistance of bare GCE. However, after PDA-Lac composite was immobilized on the GCE, the semicircle diameter (curve (b)) was apparently increased; the Ret value is around 330 Ω. This demonstrates that the interface resistance of PDA-Lac/GCE is increased in comparison with that of bare GCE because of the poor conductivity of PDA-Lac composite. While, for the PDA-Lac-rGO-Pd/GCE, the semicircle diameter (curve (c)) is decreased to some extent, the Ret value is reduced to about 200 Ω. This phenomenon can be explained by the fact that the electronic conduction ability of PDA-Lac-rGO-Pd composite was improved by the addition of rGO-Pd with good conductivity.

Figure 5(a) compares the electrocatalytic performances of different electrodes toward 220 µM catechol in 0.1 M pH 5.0 acetate buffer solution by using cyclic voltammetry. Bare GCE (curve ) shows a pair of redox peaks, which are located at around 0.47 V and 0.16 V, respectively, indicating the electrochemical redox reaction of catechol on the surface of bare GCE. Compared with bare GCE, the redox peaks of PDA/GCE (curve ) are decreased to some extent, which may be caused by the inhibiting effect of PDA layer toward electron transfer. Nevertheless, due to high-efficient catalysis of Lac toward catechol, not only the anodic peak but also the cathodic peak of PDA-Lac/GCE (curve (3)) possesses higher current value than those of bare GCE and PDA/GCE. It is noticeable that the anodic peak current and cathodic peak current of PDA-Lac-rGO/GCE (curve (4)) are increased by around 0.83 µA and 0.77 µA as compared to those of PDA-Lac/GCE, respectively. This demonstrates that addition of rGO accelerates the electron transfer of electrode, further leading to higher response sensitivity of modified electrode to catechol. A pair of redox peaks are observed on PDA-Lac-rGO-Pd/GCE (curve (5)); the anodic peak and cathodic peak are located at about 0.43 V and 0.20 V, respectively. In addition, the anodic peak current and cathodic peak current are 9.78 µA and −7.79 µA, respectively, which are higher than those of PDA-Lac-rGO/GCE, suggesting the higher sensitivity of PDA-Lac-rGO-Pd/GCE. This can be attributed to the larger number of electroactive sites of rGO-Pd offered by Pd nanoparticles and synergetic catalysis of Pd nanoparticles. The whole electrochemical reaction is a quasi-reversible cyclic process and the sensing mechanism of Lac on PDA-Lac-rGO-Pd/GCE is illustrated in Figure 1(b). Under the presence of molecular oxygen, catechol is oxidized to 1,2-benzoquinone by Lac, coupled with the electrocatalytic reduction of oxygen to water on the surface of GCE. The reaction process can be described as follows:

Figure 5(b) shows influence of scan rate on cyclic voltammograms of PDA-Lac-rGO-Pd/GCE in 0.1 M acetate buffer solution (pH 5.0) containing 220 µM catechol. The oxidation peaks (anodic peaks) and reduction peaks (cathodic peaks) simultaneously increase with the increment of scan rates. As shown in the inset of Figure 5(b), both of oxidation peak currents and reduction peak currents grow linearly with the scan rate and are proportional to the scan rates. It means that the electrochemical reaction is a surface-controlled process at PDA-Lac-rGO-Pd/GCE.

3.3. Condition Optimization

To acquire the optimum analytic performance, the test environment including solution pH and applied work potentials was optimized before the chronoamperometry experiment, and the result is shown in Figure 6. Obviously, the highest catalytic response currents happen when the solution pH is 5.0 and applied potential is 0.5 V, respectively. So, in the following experiments, these two parameter values were chosen as the fixed values.

3.4. Amperometric Analysis of Catechol

The steady-state amperometric responses of the PDA-Lac-rGO-Pd/GCE to different concentration of catechol were determined by the successive addition of different volumes of 0.2 mM, 2 mM, and 20 mM catechol into 20 mL pH 5.0 acetate buffer solution with stirring under the optimum conditions; the result is shown in Figure 7(a). It can be seen from the inset of Figure 7(a) that the first current step occurred when 2 nM of catechol was added into acetate buffer solution, indicating high sensitivity and low detection limit of PDA-Lac-rGO-Pd/GCE toward catechol. It is noticeable that the step current can reach 95% of its maximum value within 5 s, indicating the fast response of biosensor, which can be explained by the fact that the porous structure of PDA-Lac-rGO-Pd composite is favorable to the fast transfer of electrons. With the successive addition of catechol into solution, the steady-state current values gradually increased. Figure 7(b) shows the calibration curve of response currents versus substrate concentrations; the response currents increase linearly with the catechol concentrations. The linear range is from 0.1 µM to 263 µM with a correlation coefficient () of 0.983 (). The sensitivity is 18.4 µA mM−1 and the detection limit is estimated to be 0.03 µM at a signal-to-noise ratio of 3 (). Table 1 shows biosensing performance comparison of different Laccase modified electrodes toward catechol. It can be clearly seen that the PDA-Lac-rGO-Pd/GCE possesses satisfactory biosensing property toward catechol with low detection limit, high sensitivity, and wide linear range.

ElectrodesDetection limit (µM)Linear range (µM)Sensitivity (µA mM−1)Reference

PDA-Lac-rGO-Pb/GCE0.030.1–26318.4This work

The dashes in the table represent values that were not reported in the references.
3.5. Selectivity and Stability of Biosensor

The repeatability, reproducibility, anti-interference, and stability of PDA-Lac-rGO-Pd/GCE were also investigated. The relative standard deviation (RSD) value for 8 successive measurements is 1.6%, implying good repeatability. To study the reproducibility of biosensor, five PDA-Lac-rGO-Pd/GCE were, respectively, prepared under the same condition and the RSD value is calculated to be 3.2%, which demonstrated that the PDA-Lac-rGO-Pd/GCE possessed acceptable reproducibility. Figure 8(a) shows the catalytic response current of PDA-Lac-rGO-Pd/GCE toward different substances with same concentrations (6 µM), including catechol, hydroquinone, catechin, gallic acid, guaiacol, phenol, and aminophenol. No obvious interference of these interferences to catechol detection can be observed, indicating the anti-interference of PDA-Lac-rGO-Pd/GCE. Figure 8(b) displays the long-term storage stability of PDA-Lac-rGO-Pd/GCE in 0.1 M acetate buffer solution (pH 5.0) at 4°C. Through a long-term (30 days) storage, the current response value of PDA-Lac-rGO-Pd/GCE still maintained 94.1% of initial value, indicating the excellent stability of PDA-Lac-rGO-Pd/GCE, which may be attributed to the fact that the activity of Lac was well maintained by the biocompatible microenvironment provided by the PDA-rGO-Pd matrix. These results demonstrate that the PDA-Lac-rGO-Pd/GCE possesses good repeatability, reproducibility, anti-interference, and stability.

3.6. Real Sample Analysis

The practical application of the PDA-Lac-rGO-Pd/GCE biosensor was also investigated by using untreated water from Taihu Lake, Wuxi, China. Herein, recovery experiment was used and repeated for five times. The analytical results are shown in Table 2. The recovery values for five tests are 104.5%, 98.5%, 101%, 96.5%, and 98%, respectively, and the RSD for these values is only 3.14%, demonstrating the successful application of the novel PDA-Lac-rGO-Pd/GCE biosensor in real water sample analysis.

Sample (µM) (µM)Recovery (%)RSD (%)


1: Taihu Lake water.

4. Conclusions

In summary, rGO-Pd hybrid was facilely synthesized by a simple method. PDA-Lac-rGO-Pd composite was prepared by a one-pot Lac-catalyzed oxidation of DA in an aqueous suspension containing Lac, rGO-Pd, and DA. A novel biosensor based on the PDA-Lac-rGO-Pd composite was fabricated. Consequently, the biosensor showed excellent biological electrocatalysis toward phenolic pollutant, catechol, with low detection limit, high sensitivity, and wide linear range, as well as good repeatability, reproducibility, anti-interference, and stability. The biosensor was also successfully applied in catechol detection in lake water. This novel composite based on rGO further expands the application of graphene materials in the field of biosensing and paves the way in developing highly sensitive phenolic biosensor.

Competing Interests

The authors declare that they have no competing interests.


This research was financially supported by the Priority Academic Program Development of Jiangsu Higher Education Institutions, Six Talent Peaks Project in Jiangsu Province (2014-XCL001), the Fundamental Research Funds for the Central Universities (JUSRP51505 and JUSRP51621A), the Innovation Program for Graduate Education in Jiangsu Province (CXZZ13_07), and Scientific Research Foundation Program for PhD in Jiangnan University (JUDCF13022).


  1. S. Singh, D. V. S. Jain, and M. L. Singla, “Sol-gel based composite of gold nanoparticles as matix for tyrosinase for amperometric catechol biosensor,” Sensors & Actuators B: Chemical, vol. 182, pp. 161–169, 2013. View at: Publisher Site | Google Scholar
  2. A. A. Ensafi, M. Amini, and B. Rezaei, “Assessment of genotoxicity of catecholics using impedimetric DNA-biosensor,” Biosensors and Bioelectronics, vol. 53, pp. 43–50, 2014. View at: Publisher Site | Google Scholar
  3. J. Barek, H. Ebertová, V. Mejstřík, and J. Zima, “Determination of 2-nitrophenol, 4-nitrophenol, 2-methoxy-5-nitrophenol, and 2,4-dinitrophenol by differential pulse voltammetry and adsorptive stripping voltammetry,” Collection of Czechoslovak Chemical Communications, vol. 59, no. 8, pp. 1761–1771, 1994. View at: Publisher Site | Google Scholar
  4. R. E. Clement, G. A. Eiceman, and C. J. Koester, “Environmental-analysis,” Analytical Chemistry, vol. 67, no. 12, pp. R221–R255, 1995. View at: Publisher Site | Google Scholar
  5. X.-H. Zhou, L.-H. Liu, X. Bai, and H.-C. Shi, “A reduced graphene oxide based biosensor for high-sensitive detection of phenols in water samples,” Sensors and Actuators B: Chemical, vol. 181, pp. 661–667, 2013. View at: Publisher Site | Google Scholar
  6. T. Shimomura, T. Itoh, T. Sumiya, T.-A. Hanaoka, F. Mizukami, and M. Ono, “Amperometric detection of phenolic compounds with enzyme immobilized in mesoporous silica prepared by electrophoretic deposition,” Sensors and Actuators B: Chemical, vol. 153, no. 2, pp. 361–368, 2011. View at: Publisher Site | Google Scholar
  7. D. Brondani, B. de Souza, B. S. Souza, A. Neves, and I. C. Vieira, “PEI-coated gold nanoparticles decorated with laccase: a new platform for direct electrochemistry of enzymes and biosensing applications,” Biosensors and Bioelectronics, vol. 42, no. 1, pp. 242–247, 2013. View at: Publisher Site | Google Scholar
  8. X. Chen, D. Li, G. Li et al., “Facile fabrication of gold nanoparticle on zein ultrafine fibers and their application for catechol biosensor,” Applied Surface Science, vol. 328, pp. 444–452, 2015. View at: Publisher Site | Google Scholar
  9. P. M. Ajayan, “Nanotubes from Carbon,” Chemical Reviews, vol. 99, no. 7, pp. 1787–1800, 1999. View at: Publisher Site | Google Scholar
  10. A. Trifonov, R. Tel-Vered, M. Fadeev, A. Cecconello, and I. Willner, “Metal nanoparticle-loaded mesoporous carbon nanoparticles: electrical contacting of redox proteins and electrochemical sensing applications,” Electroanalysis, vol. 27, no. 9, pp. 2150–2157, 2015. View at: Publisher Site | Google Scholar
  11. S. V. Morozov, A. K. Geim, I. V. Crigorieva et al., “Electric field effect in atomically thin carbon films,” Science, vol. 306, no. 5696, pp. 666–669, 2004. View at: Publisher Site | Google Scholar
  12. C.-L. Sun, J.-S. Su, S.-Y. Lai, and Y.-J. Lu, “Size effects of Pt nanoparticle/graphene composite materials on the electrochemical sensing of hydrogen peroxide,” Journal of Nanomaterials, vol. 2015, Article ID 861061, 7 pages, 2015. View at: Publisher Site | Google Scholar
  13. A. A. Ensafi, M. Sohrabi, M. Jafari-Asl, and B. Rezaei, “Selective and sensitive furazolidone biosensor based on DNA-modified TiO2-reduced graphene oxide,” Applied Surface Science, vol. 356, pp. 301–307, 2015. View at: Publisher Site | Google Scholar
  14. L.-M. Lu, H.-B. Li, F. Qu, X.-B. Zhang, G.-L. Shen, and R.-Q. Yu, “In situ synthesis of palladium nanoparticle-graphene nanohybrids and their application in nonenzymatic glucose biosensors,” Biosensors and Bioelectronics, vol. 26, no. 8, pp. 3500–3504, 2011. View at: Publisher Site | Google Scholar
  15. S. Nandini, S. Nalini, R. Manjunatha, S. Shanmugam, J. S. Melo, and G. S. Suresh, “Electrochemical biosensor for the selective determination of hydrogen peroxide based on the co-deposition of palladium, horseradish peroxidase on functionalized-graphene modified graphite electrode as composite,” Journal of Electroanalytical Chemistry, vol. 689, pp. 233–242, 2013. View at: Publisher Site | Google Scholar
  16. Q. Zeng, J.-S. Cheng, X.-F. Liu, H.-T. Bai, and J.-H. Jiang, “Palladium nanoparticle/chitosan-grafted graphene nanocomposites for construction of a glucose biosensor,” Biosensors and Bioelectronics, vol. 26, no. 8, pp. 3456–3463, 2011. View at: Publisher Site | Google Scholar
  17. Y. Li, C. Qin, C. Chen, Y. Fu, M. Ma, and Q. Xie, “Highly sensitive phenolic biosensor based on magnetic polydopamine-laccase- Fe3O4 bionanocomposite,” Sensors and Actuators B: Chemical, vol. 168, pp. 46–53, 2012. View at: Publisher Site | Google Scholar
  18. D. Li, L. Luo, Z. Pang et al., “Novel phenolic biosensor based on a magnetic polydopamine-laccase-nickel nanoparticle loaded carbon nanofiber composite,” ACS Applied Materials and Interfaces, vol. 6, no. 7, pp. 5144–5151, 2014. View at: Publisher Site | Google Scholar
  19. Y. Fu, P. Li, Q. Xie et al., “One-pot preparation of polymer-enzyme-metallic nanoparticle composite films for high-performance biosensing of glucose and galactose,” Advanced Functional Materials, vol. 19, no. 11, pp. 1784–1791, 2009. View at: Publisher Site | Google Scholar
  20. C. Gan, L. Ling, Z. He, H. Lei, and Y. Liu, “In-situ assembly of biocompatible core-shell hierarchical nanostructures sensitized immunosensor for microcystin-LR detection,” Biosensors and Bioelectronics, vol. 78, pp. 381–389, 2016. View at: Publisher Site | Google Scholar
  21. S. H. Liu, Z. Y. Zhang, S. W. Zhou, L.-P. Jiang, and J.-J. Zhu, “An electrochemical-TUNEL method for sensitive detection of apoptotic cells,” Analyst, vol. 141, no. 2, pp. 567–569, 2016. View at: Publisher Site | Google Scholar
  22. W. S. Hummers Jr. and R. E. Offeman, “Preparation of graphitic oxide,” Journal of the American Chemical Society, vol. 80, no. 6, p. 1339, 1958. View at: Publisher Site | Google Scholar
  23. Y. Li, X. Fan, J. Qi et al., “Palladium nanoparticle-graphene hybrids as active catalysts for the Suzuki reaction,” Nano Research, vol. 3, no. 6, pp. 429–437, 2010. View at: Publisher Site | Google Scholar
  24. X. Fan, W. Peng, L. Yang et al., “Deoxygenation of exfoliated graphite oxide under alkaline conditions: a green route to graphene preparation,” Advanced Materials, vol. 20, no. 23, pp. 4490–4493, 2008. View at: Publisher Site | Google Scholar
  25. N. Karousis, G.-E. Tsotsou, F. Evangelista, P. Rudolf, N. Ragoussis, and N. Tagmatarchis, “Carbon nanotubes decorated with palladium nanoparticles: synthesis, characterization, and catalytic activity,” Journal of Physical Chemistry C, vol. 112, no. 35, pp. 13463–13469, 2008. View at: Publisher Site | Google Scholar
  26. S. K. Basiruddin and S. K. Swain, “Phenylboronic acid functionalized reduced graphene oxide based fluorescence nano sensor for glucose sensing,” Materials Science and Engineering: C, vol. 58, pp. 103–109, 2016. View at: Publisher Site | Google Scholar
  27. M. Wojtoniszak, X. Chen, R. J. Kalenczuk et al., “Synthesis, dispersion, and cytocompatibility of graphene oxide and reduced graphene oxide,” Colloids and Surfaces B: Biointerfaces, vol. 89, no. 1, pp. 79–85, 2012. View at: Publisher Site | Google Scholar
  28. K. F. Babu, B. Rajagopalan, J. S. Chung, and W. M. Choi, “Facile synthesis of graphene/N-doped carbon nanowire composites as an effective electrocatalyst for the oxygen reduction reaction,” International Journal of Hydrogen Energy, vol. 40, no. 21, pp. 6827–6834, 2015. View at: Publisher Site | Google Scholar
  29. H. Na, L. Zhang, H. Qiu et al., “A two step method to synthesize palladium-copper nanoparticles on reduced graphene oxide and their extremely high electrocatalytic activity for the electrooxidation of methanol and ethanol,” Journal of Power Sources, vol. 288, pp. 160–167, 2015. View at: Publisher Site | Google Scholar
  30. F. Tuinstra and J. L. Koenig, “Raman spectrum of graphite,” Journal of Chemical Physics, vol. 53, no. 3, pp. 1126–1130, 1970. View at: Publisher Site | Google Scholar
  31. M. Cheng, R. Yang, L. Zhang et al., “Restoration of graphene from graphene oxide by defect repair,” Carbon, vol. 50, no. 7, pp. 2581–2587, 2012. View at: Publisher Site | Google Scholar
  32. D. Yang, A. Velamakanni, G. Bozoklu et al., “Chemical analysis of graphene oxide films after heat and chemical treatments by X-ray photoelectron and Micro-Raman spectroscopy,” Carbon, vol. 47, no. 1, pp. 145–152, 2009. View at: Publisher Site | Google Scholar
  33. K. N. Kudin, B. Ozbas, H. C. Schniepp, R. K. Prud'Homme, I. A. Aksay, and R. Car, “Raman spectra of graphite oxide and functionalized graphene sheets,” Nano Letters, vol. 8, no. 1, pp. 36–41, 2008. View at: Publisher Site | Google Scholar
  34. P. An, F. Zuo, Y. P. Wu et al., “Fast synthesis of dopamine-coated Fe3O4 nanoparticles through ligand-exchange method,” Chinese Chemical Letters, vol. 23, no. 9, pp. 1099–1102, 2012. View at: Publisher Site | Google Scholar
  35. I. M. Dugandžić, D. J. Jovanović, L. T. Mančić et al., “Ultrasonic spray pyrolysis of surface modified TiO2 nanoparticles with dopamine,” Materials Chemistry and Physics, vol. 143, no. 1, pp. 233–239, 2013. View at: Publisher Site | Google Scholar
  36. M. Mazur, A. Krywko-Cendrowska, P. Krysiński, and J. Rogalski, “Encapsulation of laccase in a conducting polymer matrix: a simple route towards polypyrrole microcontainers,” Synthetic Metals, vol. 159, no. 17-18, pp. 1731–1738, 2009. View at: Publisher Site | Google Scholar
  37. K. Wang, J. Tang, Z. Zhang, Y. Gao, and G. Chen, “Laccase on Black Pearl 2000 modified glassy carbon electrode: characterization of direct electron transfer and biological sensing properties for pyrocatechol,” Electrochimica Acta, vol. 70, pp. 112–117, 2012. View at: Publisher Site | Google Scholar
  38. Y. Zhou, L. Tang, G. Zeng et al., “Mesoporous carbon nitride based biosensor for highly sensitive and selective analysis of phenol and catechol in compost bioremediation,” Biosensors and Bioelectronics, vol. 61, pp. 519–525, 2014. View at: Publisher Site | Google Scholar
  39. X. Xu, P. Lu, Y. Zhou, Z. Zhao, and M. Guo, “Laccase immobilized on methylene blue modified mesoporous silica MCM-41/PVA,” Materials Science and Engineering C, vol. 29, no. 7, pp. 2160–2164, 2009. View at: Publisher Site | Google Scholar
  40. X. Xu, M. Guo, P. Lu, and R. Wang, “Development of amperometric laccase biosensor through immobilizing enzyme in copper-containing ordered mesoporous carbon (Cu-OMC)/chitosan matrix,” Materials Science and Engineering: C, vol. 30, no. 5, pp. 722–729, 2010. View at: Publisher Site | Google Scholar
  41. T. Shimomura, T. Itoh, T. Sumiya, T.-A. Hanaoka, F. Mizukami, and M. Ono, “Amperometric detection of phenolic compounds with enzyme immobilized in mesoporous silica prepared by electrophoretic deposition,” Sensors and Actuators, B: Chemical, vol. 153, no. 2, pp. 361–368, 2011. View at: Publisher Site | Google Scholar
  42. J. Fu, H. Qiao, D. Li, L. Luo, K. Chen, and Q. Wei, “Laccase biosensor based on electrospun copper/carbon composite nanofibers for catechol detection,” Sensors, vol. 14, no. 2, pp. 3543–3556, 2014. View at: Publisher Site | Google Scholar
  43. X. Y. Wang, M. M. Xi, M. M. Guo et al., “An electrochemically aminated glassy carbon electrode for simultaneous determination of hydroquinone and catechol,” Analyst, vol. 141, no. 3, pp. 1077–1082, 2016. View at: Publisher Site | Google Scholar
  44. F. Campanhã Vicentini, L. L. C. Garcia, L. C. S. Figueiredo-Filho, B. C. Janegitz, and O. Fatibello-Filho, “A biosensor based on gold nanoparticles, dihexadecylphosphate, and tyrosinase for the determination of catechol in natural water,” Enzyme and Microbial Technology, vol. 84, pp. 17–23, 2016. View at: Publisher Site | Google Scholar

Copyright © 2016 Da-Wei Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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